162 related articles for article (PubMed ID: 10998140)
1. Assignment of the gene for a new hereditary nail disorder, isolated congenital nail dysplasia, to chromosome 17p13.
Krebsová A; Hamm H; Karl S; Reis A; Hennies HC
J Invest Dermatol; 2000 Oct; 115(4):664-7. PubMed ID: 10998140
[TBL] [Abstract][Full Text] [Related]
2. Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2.
Naeem M; Jelani M; Lee K; Ali G; Chishti MS; Wali A; Gul A; John P; Hassan MJ; Leal SM; Ahmad W
Br J Dermatol; 2006 Dec; 155(6):1184-90. PubMed ID: 17107387
[TBL] [Abstract][Full Text] [Related]
3. Hereditary 'white nails': a genetic and structural study.
Norgett EE; Wolf F; Balme B; Leigh IM; Perrot H; Kelsell DP; Haftek M
Br J Dermatol; 2004 Jul; 151(1):65-72. PubMed ID: 15270873
[TBL] [Abstract][Full Text] [Related]
4. Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3.
Rafiq MA; Ansar M; Pham T; Amin-ud-Din M; Anwar M; Haque S; Chahrour MH; Yan K; Leal SM; Ahmad W
Clin Genet; 2004 Jul; 66(1):73-8. PubMed ID: 15200512
[TBL] [Abstract][Full Text] [Related]
5. Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
Tariq M; Azeem Z; Ali G; Chishti MS; Ahmad W
J Med Genet; 2009 Jan; 46(1):14-20. PubMed ID: 18805827
[TBL] [Abstract][Full Text] [Related]
6. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
Tariq M; Chishti MS; Ali G; Ahmad W
Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143
[TBL] [Abstract][Full Text] [Related]
7. Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.
Naeem M; John P; Ali G; Ahmad W
Clin Exp Dermatol; 2007 Sep; 32(5):502-5. PubMed ID: 17489990
[TBL] [Abstract][Full Text] [Related]
8. A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.
Naeem M; Wajid M; Lee K; Leal SM; Ahmad W
J Med Genet; 2006 Mar; 43(3):274-9. PubMed ID: 16525032
[TBL] [Abstract][Full Text] [Related]
9. Isolated congenital nail dysplasia: a new autosomal dominant condition.
Hamm H; Karl S; Bröcker EB
Arch Dermatol; 2000 Oct; 136(10):1239-43. PubMed ID: 11030770
[TBL] [Abstract][Full Text] [Related]
10. The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21.
Whittock NV; Coleman CM; McLean WH; Ashton GH; Acland KM; Eady RA; McGrath JA
J Invest Dermatol; 2000 Oct; 115(4):694-8. PubMed ID: 10998145
[TBL] [Abstract][Full Text] [Related]
11. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation.
Rasool M; Nawaz S; Azhar A; Wajid M; Westermark P; Baig SM; Klar J; Dahl N
Eur J Dermatol; 2010; 20(4):443-6. PubMed ID: 20409997
[TBL] [Abstract][Full Text] [Related]
12. A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31.
Habib R; Ansar M; Mattheisen M; Shahid M; Ali G; Ahmad W; Betz RC
PLoS One; 2015; 10(6):e0129811. PubMed ID: 26115030
[TBL] [Abstract][Full Text] [Related]
13. A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.
Hameed A; Khaliq S; Ismail M; Anwar K; Ebenezer ND; Jordan T; Mehdi SQ; Payne AM; Bhattacharya SS
Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):629-33. PubMed ID: 10711674
[TBL] [Abstract][Full Text] [Related]
14. Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity.
Birch-Machin MA; Healy E; Turner R; Haldane F; Belgaid CE; Darlington S; Stephenson AM; Munro C; Messenger AG; Rees JL
Br J Dermatol; 1997 Sep; 137(3):339-43. PubMed ID: 9349326
[TBL] [Abstract][Full Text] [Related]
15. A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
Munro CS; Carter S; Bryce S; Hall M; Rees JL; Kunkeler L; Stephenson A; Strachan T
J Med Genet; 1994 Sep; 31(9):675-8. PubMed ID: 7529318
[TBL] [Abstract][Full Text] [Related]
16. A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13.
Healy E; Holmes SC; Belgaid CE; Stephenson AM; Mclean WH; Rees JL; Munro CS
Hum Mol Genet; 1995 Dec; 4(12):2399-402. PubMed ID: 8634717
[TBL] [Abstract][Full Text] [Related]
17. Dizygotic twins with congenital malalignment of the great toenails: reappraisal of the pathogenesis.
Chaniotakis I; Bonitsis N; Stergiopoulou C; Kiorpelidou D; Bassukas ID
J Am Acad Dermatol; 2007 Oct; 57(4):711-5. PubMed ID: 17692994
[TBL] [Abstract][Full Text] [Related]
18. Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literature.
Kasparis C; Reid D; Wilson NJ; Okur V; Cole C; Hansen CD; Bosse K; Betz RC; Khan M; Smith FJ
Clin Exp Dermatol; 2016 Dec; 41(8):884-889. PubMed ID: 27786367
[TBL] [Abstract][Full Text] [Related]
19. Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22.
Mangino M; Sanchez O; Torrente I; De Luca A; Capon F; Novelli G; Dallapiccola B
Am J Hum Genet; 1999 Aug; 65(2):441-7. PubMed ID: 10417287
[TBL] [Abstract][Full Text] [Related]
20. Hereditary hypodontia and onychorrhexis of the fingernails and toenail koilonychia: Witkop's tooth-and nail syndrome.
Zabawski EJ; Cohen JB
Dermatol Online J; 1999 May; 5(1):3. PubMed ID: 10673446
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
